Perioperative Rehabilitation in Operation for Lung Cancer (PROLUCA)
Primary Purpose
Lung Cancer, Non Small Cell Lung Cancer
Status
Terminated
Phase
Not Applicable
Locations
Denmark
Study Type
Interventional
Intervention
Experimental: 1. Experimental
Experimental: 2. Experimental
Experimental: 3. Experimental
Other: 4. Usual care
Sponsored by

About this trial
This is an interventional treatment trial for Lung Cancer focused on measuring Cancer, Rehabilitation, Exercise, Lung cancer, NSCLC
Eligibility Criteria
Inclusion Criteria:
- Performance status 0-2 (WHO)
- Living in the City of Copenhagen or surrounding Municipalities
- Ability to read and understand Danish
- Approval by primary surgeon
Exclusion Criteria:
- Presence of metastatic disease or surgical inoperability
- Diagnosis of Lung Cancer not verified by histological diagnosis
- Cardiac disease
Sites / Locations
- Copenhagen Centre for Cancer and Health
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm 4
Arm Type
Experimental
Experimental
Experimental
Other
Arm Label
1. Experimental
2. Experimental
3. Experimental
4. Usual care
Arm Description
Home-based exercise pre surgery and postoperative exercise in a team initiated two weeks after surgery.
Home-based exercise pre surgery and postoperative exercise in a team initiated six weeks after surgery.
Exercise in a team initiated two weeks after surgery.
Exercise in a team initiated six weeks after surgery.
Outcomes
Primary Outcome Measures
Maximum oxygen uptake (VO2peak)
VO2peak is evaluated by an incremental test using an electromagnetically braked cycle ergometer (Lode Corival Ergometer©). Inspired and expired gases are analyzed breath-by-breath by a metabolic cart (JAEGER MasterScreen CPX©). Subjects begin pedaling at seven watts and resistance increases after a predefined 10 watts ramp protocol until exhaustion or a symptom-limited VO2peak is achieved (pain, dizziness, anxiety etc.).
Secondary Outcome Measures
Six minute walk distance (6MWD)
Patient reported outcomes (PROs)
PROs will include health related quality of life, symptoms and side-effects, anxiety and depression, well-being, distress, lifestyle, sickness absence, work status, and social support.
Pulmonary function
forced expiratory volume at one second
Full Information
NCT ID
NCT01893580
First Posted
June 20, 2013
Last Updated
May 5, 2015
Sponsor
Rigshospitalet, Denmark
Collaborators
Centre for Integrated Rehabilitation of Cancer patients, CIRE, Denmark, Danish Cancer Society, Novo Nordisk A/S, University of Copenhagen, Copenhagen Centre for Cancer and Health, Denmark.
1. Study Identification
Unique Protocol Identification Number
NCT01893580
Brief Title
Perioperative Rehabilitation in Operation for Lung Cancer
Acronym
PROLUCA
Official Title
Perioperative Rehabilitation in Operation for Lung Cancer
Study Type
Interventional
2. Study Status
Record Verification Date
May 2015
Overall Recruitment Status
Terminated
Why Stopped
Due to low recruiment rate, the study design is chanced to a feasibility study
Study Start Date
May 2012 (undefined)
Primary Completion Date
October 2014 (Actual)
Study Completion Date
January 2015 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Rigshospitalet, Denmark
Collaborators
Centre for Integrated Rehabilitation of Cancer patients, CIRE, Denmark, Danish Cancer Society, Novo Nordisk A/S, University of Copenhagen, Copenhagen Centre for Cancer and Health, Denmark.
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Background: Improved surgical techniques combined with effective adjuvant chemotherapy, has led to a better survival in individuals with NSCLC. The treatment of NSCLC and other cancer diseases are after all still complex and potentially lethal.
Study aim: The rationale for the study PROLUCA is to identify the optimal timing of exercise to improve recovery after surgery in patients operated for lunge cancer with focus on physical capacity and quality of life.
Who can participate? Patients above 18 years and diagnosed with lung cancer and referred for operation. Participation in this study is not possible if the participants by a doctor are advised not to do strenuous exercise.
What does the study involve? The intervention consists of a combination of (1) exercise before surgery and (2) exercise after surgery for lung cancer.
Exercise before surgery is a home-based exercise program is individually designed and must be performed for at least 30 minutes every day until surgery. The home-based exercise program varies in length due to number of days until surgery, and the intention is not exceed 14 days.
The exercise initiated two weeks and 6 weeks after surgery consists of a 12 weeks rehabilitation program and three individual counseling sessions. Special needs in terms of smoking cessation, nutritional counseling or patient education, this is also offered. The exercise consists of individually prepared supervised strength - and fitness exercise in a team, two sessions of 60 minutes/week.
What interventions will be compared? A home-based post-operative exercise program, combined with exercise initiated two weeks after surgery, will be compared with usual care (exercise initiated six weeks after surgery).
Will all participants receive the same treatment?
By draw it is decided which of the 4 groups the participants will attend to in the study:
Group 1: Home-based exercise before surgery and rehabilitation initiated as early as two weeks after surgery
Group 2: Home-based exercise before surgery and rehabilitation initiated six weeks after surgery
Group 3: Rehabilitation initiated as early as two weeks after surgery
Group 4: Rehabilitation initiated six weeks after surgery (Usual practice as control group) What are the possible benefits and risks of participating? There are no risks or side- effects of participating other than muscle soreness and exercise is beneficial when it comes to recover from an operation from lung cancer.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Lung Cancer, Non Small Cell Lung Cancer
Keywords
Cancer, Rehabilitation, Exercise, Lung cancer, NSCLC
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Care ProviderOutcomes Assessor
Allocation
Randomized
Enrollment
40 (Actual)
8. Arms, Groups, and Interventions
Arm Title
1. Experimental
Arm Type
Experimental
Arm Description
Home-based exercise pre surgery and postoperative exercise in a team initiated two weeks after surgery.
Arm Title
2. Experimental
Arm Type
Experimental
Arm Description
Home-based exercise pre surgery and postoperative exercise in a team initiated six weeks after surgery.
Arm Title
3. Experimental
Arm Type
Experimental
Arm Description
Exercise in a team initiated two weeks after surgery.
Arm Title
4. Usual care
Arm Type
Other
Arm Description
Exercise in a team initiated six weeks after surgery.
Intervention Type
Behavioral
Intervention Name(s)
Experimental: 1. Experimental
Other Intervention Name(s)
Preoperative and early postoperative rehabilitation
Intervention Description
Home-based exercise pre surgery and postoperative exercise in a team initiated two weeks after surgery. Intervention consists of:
Preoperative home-based exercise program - cardiovascular exercise of moderate-vigorous intensity for at least 30 minutes every day until surgery.
Postoperative rehabilitation: A supervised 12-week rehabilitation program containing 24 group-based exercise sessions, three individual counseling sessions and smoking cessation, nutritional counseling or patient education, this is offered too.The cardiorespiratory intensity is at ~50-60% of individual HRmax for the first four weeks and increases to moderate-high intensity at ~70-90% of individually determined HRmax. The intensity of the strength exercise program is at ~60-80% of 1 RM.
Intervention Type
Behavioral
Intervention Name(s)
Experimental: 2. Experimental
Other Intervention Name(s)
Preoperative and late postoperative rehabilitation
Intervention Description
Home-based exercise pre surgery and postoperative exercise in a team initiated six weeks after surgery. Intervention consists of:
Preoperative home-based exercise program - cardiovascular exercise of moderate-vigorous intensity for at least 30 minutes every day until surgery.
Postoperative rehabilitation: A supervised 12-week rehabilitation program containing 24 group-based exercise sessions, three individual counseling sessions and smoking cessation, nutritional counseling or patient education, this is offered too.The cardiorespiratory intensity is at ~50-60% of individual HRmax for the first four weeks and increases to moderate-high intensity at ~70-90% of individually determined HRmax. The intensity of the strength exercise program is at ~60-80% of 1 RM.
Intervention Type
Behavioral
Intervention Name(s)
Experimental: 3. Experimental
Other Intervention Name(s)
Early postoperative rehabilitation alone
Intervention Description
Early postoperative exercise in a team initiated two weeks after surgery. Intervention consists of:
Postoperative rehabilitation: A supervised 12-week rehabilitation program containing 24 group-based exercise sessions, three individual counseling sessions and smoking cessation, nutritional counseling or patient education, this is offered too.The cardiorespiratory intensity is at ~50-60% of individual HRmax for the first four weeks and increases to moderate-high intensity at ~70-90% of individually determined HRmax. The intensity of the strength exercise program is at ~60-80% of 1 RM.
Intervention Type
Behavioral
Intervention Name(s)
Other: 4. Usual care
Other Intervention Name(s)
Usual care
Intervention Description
Exercise in a team initiated six weeks after surgery consisting of a supervised 12-week rehabilitation program containing 24 group-based exercise sessions, three individual counseling sessions, and three group-based lessons in health-promoting behavior. If the participants have special needs in terms of smoking cessation, nutritional counseling or patient education, this is offered too.
The cardiorespiratory intensity is at ~50-60% of individual HRmax for the first four weeks. The next eight weeks the intensity increases to moderate-high intensity at ~70-90% of individually determined HRmax. The intensity of the strength exercise program is at ~60-80% of 1 RM.
Primary Outcome Measure Information:
Title
Maximum oxygen uptake (VO2peak)
Description
VO2peak is evaluated by an incremental test using an electromagnetically braked cycle ergometer (Lode Corival Ergometer©). Inspired and expired gases are analyzed breath-by-breath by a metabolic cart (JAEGER MasterScreen CPX©). Subjects begin pedaling at seven watts and resistance increases after a predefined 10 watts ramp protocol until exhaustion or a symptom-limited VO2peak is achieved (pain, dizziness, anxiety etc.).
Time Frame
VO2peak is assessed at baseline, the day before surgery, post-intervention (14/18 weeks after surgery), six months after surgery, and one year after surgery.
Secondary Outcome Measure Information:
Title
Six minute walk distance (6MWD)
Time Frame
baseline, the day before surgery, pre-intervention (2/6 weeks after surgery), post-intervention (14/18 weeks after surgery), six months after surgery, and one year after surgery.
Title
Patient reported outcomes (PROs)
Description
PROs will include health related quality of life, symptoms and side-effects, anxiety and depression, well-being, distress, lifestyle, sickness absence, work status, and social support.
Time Frame
Baseline, the day before surgery, pre-intervention (2/6 weeks after surgery), post-intervention (14/18 weeks after surgery), six months after surgery, and one year after surgery.
Title
Pulmonary function
Description
forced expiratory volume at one second
Time Frame
Baseline, the day before surgery, post-intervention (14/18 weeks after surgery), six months after surgery, and one year after surgery.
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Performance status 0-2 (WHO)
Living in the City of Copenhagen or surrounding Municipalities
Ability to read and understand Danish
Approval by primary surgeon
Exclusion Criteria:
Presence of metastatic disease or surgical inoperability
Diagnosis of Lung Cancer not verified by histological diagnosis
Cardiac disease
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jesper Holst Pedersen, MD, DrMSci
Organizational Affiliation
Department of Cardiothoracic Surgery RT
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Jette Vibe-Petersen, MD
Organizational Affiliation
Copenhagen Centre for Cancer and Health
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Maja Schick Sommer, MHS
Organizational Affiliation
Copenhagen Centre for Cancer and Health
Official's Role
Principal Investigator
Facility Information:
Facility Name
Copenhagen Centre for Cancer and Health
City
Copenhagen
State/Province
Nørrebro
ZIP/Postal Code
DK-2200
Country
Denmark
12. IPD Sharing Statement
Citations:
PubMed Identifier
24898680
Citation
Sommer MS, Trier K, Vibe-Petersen J, Missel M, Christensen M, Larsen KR, Langer SW, Hendriksen C, Clementsen P, Pedersen JH, Langberg H. Perioperative rehabilitation in operation for lung cancer (PROLUCA) - rationale and design. BMC Cancer. 2014 Jun 4;14:404. doi: 10.1186/1471-2407-14-404.
Results Reference
derived
Learn more about this trial
Perioperative Rehabilitation in Operation for Lung Cancer
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